TY - JOUR
T1 - Kinetically blocked stable heptazethrene and octazethrene
T2 - Closed-shell or open-shell in the ground state?
AU - Li, Yuan
AU - Heng, Wee Kuan
AU - Lee, Byung Sun
AU - Aratani, Naoki
AU - Zafra, José L.
AU - Bao, Nina
AU - Lee, Richmond
AU - Sung, Young Mo
AU - Sun, Zhe
AU - Huang, Kuo Wei
AU - Webster, Richard D.
AU - López Navarrete, Juan T.
AU - Kim, Dongho
AU - Osuka, Atsuhiro
AU - Casado, Juan
AU - Ding, Jun
AU - Wu, Jishan
PY - 2012/9/12
Y1 - 2012/9/12
N2 - Polycyclic aromatic hydrocarbons with an open-shell singlet biradical ground state are of fundamental interest and have potential applications in materials science. However, the inherent high reactivity makes their synthesis and characterization very challenging. In this work, a convenient synthetic route was developed to synthesize two kinetically blocked heptazethrene (HZ-TIPS) and octazethrene (OZ-TIPS) compounds with good stability. Their ground-state electronic structures were systematically investigated by a combination of different experimental methods, including steady-state and transient absorption spectroscopy, variable temperature NMR, electron spin resonance (ESR), superconducting quantum interfering device (SQUID), FT Raman, and X-ray crystallographic analysis, assisted by unrestricted symmetry-broken density functional theory (DFT) calculations. All these demonstrated that the heptazethrene derivative HZ-TIPS has a closed-shell ground state while its octazethrene analogue OZ-TIPS with a smaller energy gap exists as an open-shell singlet biradical with a large measured biradical character (y = 0.56). Large two-photon absorption (TPA) cross sections (σ(2)) were determined for HZ-TIPS (σ(2)max = 920 GM at 1250 nm) and OZ-TIPS (σ(2)max = 1200 GM at 1250 nm). In addition, HZ-TIPS and OZ-TIPS show a closely stacked 1D polymer chain in single crystals.
AB - Polycyclic aromatic hydrocarbons with an open-shell singlet biradical ground state are of fundamental interest and have potential applications in materials science. However, the inherent high reactivity makes their synthesis and characterization very challenging. In this work, a convenient synthetic route was developed to synthesize two kinetically blocked heptazethrene (HZ-TIPS) and octazethrene (OZ-TIPS) compounds with good stability. Their ground-state electronic structures were systematically investigated by a combination of different experimental methods, including steady-state and transient absorption spectroscopy, variable temperature NMR, electron spin resonance (ESR), superconducting quantum interfering device (SQUID), FT Raman, and X-ray crystallographic analysis, assisted by unrestricted symmetry-broken density functional theory (DFT) calculations. All these demonstrated that the heptazethrene derivative HZ-TIPS has a closed-shell ground state while its octazethrene analogue OZ-TIPS with a smaller energy gap exists as an open-shell singlet biradical with a large measured biradical character (y = 0.56). Large two-photon absorption (TPA) cross sections (σ(2)) were determined for HZ-TIPS (σ(2)max = 920 GM at 1250 nm) and OZ-TIPS (σ(2)max = 1200 GM at 1250 nm). In addition, HZ-TIPS and OZ-TIPS show a closely stacked 1D polymer chain in single crystals.
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U2 - 10.1021/ja304618v
DO - 10.1021/ja304618v
M3 - Article
C2 - 22908899
AN - SCOPUS:84865801594
SN - 0002-7863
VL - 134
SP - 14913
EP - 14922
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 36
ER -